Research Participation Decision-Making Among Youth and Parents of Youth with Chronic Health Conditions: A Dissertation
Faculty AdvisorCarol Bova
UMass Chan AffiliationsGraduate School of Nursing
Document TypeDoctoral Dissertation
KeywordsChronic health conditions
Bioethics and Medical Ethics
Health Services Administration
Health Services Research
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AbstractThe purpose and aims of this qualitative descriptive study were to describe how past experiences with research (including communication, information, values and support) may contribute to research fatigue among youth and parents of youth with HIV, CF, and T1D. Eighteen parents and youth were purposively recruited from outpatient subspecialty clinics at a major academic medical center. They took part in qualitative interviews, completed a demographics form, and the Decisional Conflict Scale. Youth participants also completed the Erikson Psychosocial Stage Inventory. Two major themes emerged: blurred lines and hope for the future. Research fatigue was not found in this sample. Results point to challenges with informed consent in settings where research and clinical care are integrated, and suggest that protective factors allow for continued participation without excess burden on youth and parents. Strategies to minimize research fatigue and support engagement in research are offered.
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/34391
Material from this dissertation has been published in: Pagano-Therrien J, Sullivan-Bolyai S. Research Participation Decision-Making Among Youth and Parents of Youth With Chronic Health Conditions. J Pediatr Health Care. 2016 Aug 20. pii: S0891-5245(16)30157-2. doi: 10.1016/j.pedhc.2016.07.002. PubMed PMID: 27553117.
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Except where otherwise noted, this item's license is described as Copyright is held by the author, with all rights reserved.